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Tschantz, M.A., Burgess, L.E. and Meyers, A.I. (1996) (S)-(-)-5-Heptyl-2-pyrrolidineone. Chiral Bicyclic Lactams as Templates for Pyrrolidines and Pyrrolidinones. Organic Synthesis, 73, 221-230.

has been cited by the following article:

• TITLE: Simple Reduction of Hydantoins with Sodium Borohydride

  AUTHORS: Jun-Ichi Yamaguchi, Emiko Shibuta, Yoshie Oishi

  KEYWORDS: Hydantoin, Reduction, Imidazolidinone

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.4 No.5, December 26, 2014

  ABSTRACT: The reduction of various hydantoins with sodium borohydride gave the corresponding 4-hydroxy- 2-imidazolidinones in high yields. In contrast, reduction employing a boron trifluoride etherate-sodium borohydride system generated 2-imidazolidinones. In both reductions, the reactivity of the hydantoin was dependent on its substituents. The Lewis acid-promoted reactions of a 4-hydroxy-2-imidazolidinone with nucleophiles were also investigated.